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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2185605Generated: October 31, 2026

Heptyl acetate → HCID 12654515, compound

https://huagongshe.com/reaction/2185605

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHeptyl acetateHCID 8159—
ReactantHexafluoropropyleneHCID 8302—
ReactantFluorineHCID 24524—
ReactantPotassium FluorideHCID 522689—
ReactantHCID 86758092HCID 86758092—
SolventDiglymeHCID 8150—
ProductHCID 12654515HCID 12654515—

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture consisting of 2027 g of trifluoroacetic acid pentadecafluoroheptyl ester (made by reacting heptyl acetate with fluorine gas as described in U.S. Pat. No. 5,399,718 (Costello et al.)), 777 g of 3M™ PF-5052 Performance Liquid (a mixture of perfluorinated solvents, available from 3M Company), 3171 g of anhydrous diglyme and 79 g of anhydrous potassium fluoride were added to a 2-gallon (7.6 L) stainless steel stirred pressure vessel. The vessel was heated and 1816 g of hexafluoropropylene was added over a 2-hour period while maintaining a reaction temperature of about 50° C. The vessel was held at 50° C. for an additional 1½ hours after the hexafluoropropylene addition was complete. The reactor was cooled and drained. The resulting liquid was phase split and the lower phase fractionally distilled to give 565 g of 1,1,1,2,4,4,4-heptafluoro-3-trifluoromethyl-butan-2-one having a boiling point of 25° C. and purity of 95% and 1427 g of 1,1,1,2,4,4,5,5,6,6,7,7,8,8,9,9,9-heptadecafluoro-2-trifluoromethyl-nonan-3-one, having a boiling point of 134° C. and a 98.5% purity as determined by gas chromatography and mass spectroscopy.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06403149B1
Source datasetuspto-grants-2002_06
ORD IDord-00460807e8614b7b92b607a0e21cf453
Source noteuspto-grants-2002_06